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Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis
Corneal infections are frequent and potentially vision-threatening diseases, and despite the significance of the immunological response in animal models of microbial keratitis (MK), it remains unclear in humans. The aim of this study was to describe the cytokine profile of tears in patients with MK....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394453/ https://www.ncbi.nlm.nih.gov/pubmed/25741769 http://dx.doi.org/10.3390/ijms16034850 |
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author | Santacruz, Concepcion Linares, Marisela Garfias, Yonathan Loustaunau, Luisa M. Pavon, Lenin Perez-Tapia, Sonia Mayra Jimenez-Martinez, Maria C. |
author_facet | Santacruz, Concepcion Linares, Marisela Garfias, Yonathan Loustaunau, Luisa M. Pavon, Lenin Perez-Tapia, Sonia Mayra Jimenez-Martinez, Maria C. |
author_sort | Santacruz, Concepcion |
collection | PubMed |
description | Corneal infections are frequent and potentially vision-threatening diseases, and despite the significance of the immunological response in animal models of microbial keratitis (MK), it remains unclear in humans. The aim of this study was to describe the cytokine profile of tears in patients with MK. Characteristics of ocular lesions such as size of the epithelial defect, stromal infiltration, and hypopyon were analyzed. Immunological evaluation included determination of interleukine (IL)-1β, IL-6, IL-8, IL-10, IL-12 and tumor necrosis factor (TNF)-α in tear samples obtained from infected eyes of 28 patients with MK and compared with their contralateral non-infected eyes. Additionally, frequency of CD4(+), CD8(+), CD19(+) and CD3(−)CD56(+) cells was also determined in peripheral blood mononuclear cells in patients with MK, and compared with 48 healthy controls. Non-significant differences were observed in the size of the epithelial defect, stromal infiltration, and hypopyon. Nevertheless, we found an immunological profile apparently related to MK etiology. IL-8 > IL-6 in patients with bacterial keratitis; IL-8 > IL-6 > IL-1β and increased frequency of circulating CD3(−)CD56(+) NK cells in patients with gram-negative keratitis; and IL-8 = IL-6 > IL-1β in patients with fungal keratitis. Characterization of tear cytokines from patients with MK could aid our understanding of the immune pathophysiological mechanisms underlying corneal damage in humans. |
format | Online Article Text |
id | pubmed-4394453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43944532015-05-21 Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis Santacruz, Concepcion Linares, Marisela Garfias, Yonathan Loustaunau, Luisa M. Pavon, Lenin Perez-Tapia, Sonia Mayra Jimenez-Martinez, Maria C. Int J Mol Sci Article Corneal infections are frequent and potentially vision-threatening diseases, and despite the significance of the immunological response in animal models of microbial keratitis (MK), it remains unclear in humans. The aim of this study was to describe the cytokine profile of tears in patients with MK. Characteristics of ocular lesions such as size of the epithelial defect, stromal infiltration, and hypopyon were analyzed. Immunological evaluation included determination of interleukine (IL)-1β, IL-6, IL-8, IL-10, IL-12 and tumor necrosis factor (TNF)-α in tear samples obtained from infected eyes of 28 patients with MK and compared with their contralateral non-infected eyes. Additionally, frequency of CD4(+), CD8(+), CD19(+) and CD3(−)CD56(+) cells was also determined in peripheral blood mononuclear cells in patients with MK, and compared with 48 healthy controls. Non-significant differences were observed in the size of the epithelial defect, stromal infiltration, and hypopyon. Nevertheless, we found an immunological profile apparently related to MK etiology. IL-8 > IL-6 in patients with bacterial keratitis; IL-8 > IL-6 > IL-1β and increased frequency of circulating CD3(−)CD56(+) NK cells in patients with gram-negative keratitis; and IL-8 = IL-6 > IL-1β in patients with fungal keratitis. Characterization of tear cytokines from patients with MK could aid our understanding of the immune pathophysiological mechanisms underlying corneal damage in humans. MDPI 2015-03-03 /pmc/articles/PMC4394453/ /pubmed/25741769 http://dx.doi.org/10.3390/ijms16034850 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Santacruz, Concepcion Linares, Marisela Garfias, Yonathan Loustaunau, Luisa M. Pavon, Lenin Perez-Tapia, Sonia Mayra Jimenez-Martinez, Maria C. Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis |
title | Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis |
title_full | Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis |
title_fullStr | Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis |
title_full_unstemmed | Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis |
title_short | Expression of IL-8, IL-6 and IL-1β in Tears as a Main Characteristic of the Immune Response in Human Microbial Keratitis |
title_sort | expression of il-8, il-6 and il-1β in tears as a main characteristic of the immune response in human microbial keratitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394453/ https://www.ncbi.nlm.nih.gov/pubmed/25741769 http://dx.doi.org/10.3390/ijms16034850 |
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